Reacción #2275695

ord-0aef4643672246cb98ea1643d6be897a

Ecuación de reacción

N#Cc1ncc(OCc2ccccc2)cc1OCc1ccccc1
3,5-bis-benzyloxy-pyridine-2-carbonitrile
CO
MeOH
[Na+].[OH-]
sodium hydroxide
O=C(O)c1ncc(OCc2ccccc2)cc1OCc1ccccc1
desired product
O=C(O)c1ncc(OCc2ccccc2)cc1OCc1ccccc1
3,5-bis-benzyloxy-pyridine-2-carboxylic acid

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction mixture is refluxed for 16 hours
  2. 2
    OtroThe solvent is removed under reduced pressure
  3. 3
    OtroThe precipitate that results
  4. 4
    Filtraciónis collected by filtration
  5. 5
    Lavadowashed with H2O (10 mL)
  6. 6
    Otrodried overnight in a vacuum oven

Procedimiento

To a solution of 3,5-bis-benzyloxy-pyridine-2-carbonitrile, 1, (26.0 g, 82.3 mmol) in MeOH (217 mL) is added 30% w/v sodium hydroxide (320 mL) and the reaction mixture is refluxed for 16 hours. The solvent is removed under reduced pressure and the resulting suspension is acidified with conc. HCl until the pH is between 1 and 2. The precipitate that results is collected by filtration, washed with H2O (10 mL) and dried overnight in a vacuum oven to afford 30 g (quantitative) of the desired product as the hydrochloride salt. 1H NMR (250 MHz, DMSO-d6) δ ppm 8.02 (1H, d, J=2.4 Hz), 7.29-7.53 (11H, m), 5.96 (1H, br s), 5.28 (4H, s). HPLC-MS: m/z 336 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08323671B2uspto-grants-2012_12